Glycosyl groups

Definition: A glycosyl group is a group obtained by removing the hydroxy group from the hemiacetal function of a monosaccharide and, by extension, of a lower oligosaccharide.

ID: CHEBI:24403

Synonyms:

Articles referencing this term

Automated synthesis of lipomannan backbone α(1-6) oligomannoside via glycosyl phosphates: glycosyl tricyclic orthoesters revisited
Xinyu Liu, Reiko Wada, Siwarutt Boonyarattanakalin, Bastien Castagner and Peter H. Seeberger, Chem. Commun., 2008 , 3510
DOI: 10.1039/b804069a

Stereocontrolled synthesis of fully functionalized d-glucosamine monosaccharides via a domino nitro-Michael/Henry reaction
Alexander Adibekian, Mattie S. M. Timmer, Pierre Stallforth, Jimmy van Rijn, Daniel B. Werz and Peter H. Seeberger, Chem. Commun., 2008 , 3549
DOI: 10.1039/b805159c

Carbohydrate microarrays as powerful tools in studies of carbohydrate-mediated biological processes
Sungjin Park, Myung-Ryul Lee and Injae Shin, Chem. Commun., 2008 , 4389
DOI: 10.1039/b806699j

Gold mediated glycosylations: selective activation of propargyl 1,2-orthoesters in the presence of aglycones containing a propargyl moiety
Gopalsamy Sureshkumar and Srinivas Hotha, Chem. Commun., 2008 , 4282
DOI: 10.1039/b806707d

Glycoarrays—tools for determining protein–carbohydrate interactions and glycoenzyme specificity
Nicolas Laurent, Josef Voglmeir and Sabine L. Flitsch, Chem. Commun., 2008 , 4400
DOI: 10.1039/b806983m

Chemoenzymatic synthesis of GDP-azidodeoxymannoses: non-radioactive probes for mannosyltransferase activity
Silvia Marchesan and Derek Macmillan, Chem. Commun., 2008 , 4321
DOI: 10.1039/b807016d

Enzyme-catalyzed synthesis of isosteric phosphono-analogues of sugar nucleotides
Stephen A. Beaton, Malcolm P. Huestis, Ali Sadeghi-Khomami, Neil R. Thomas and David L. Jakeman, Chem. Commun., 2009 , 238
DOI: 10.1039/b808078j

8-Nitroguanosines as chemical probes of the protein S-guanylation
Yohei Saito, Hirobumi Taguchi, Shigemoto Fujii, Tomohiro Sawa, Eriko Kida, Chizuko Kabuto, Takaaki Akaike and Hirokazu Arimoto, Chem. Commun., 2008 , 5984
DOI: 10.1039/b810771h

Molecular recognition, fluorescence sensing, and biological assay of phosphate anion derivatives using artificial Zn(ii)–Dpa complexes
Takashi Sakamoto, Akio Ojida and Itaru Hamachi, Chem. Commun., 2009 , 141
DOI: 10.1039/b812374h

Enzyme assays
Jean-Louis Reymond, Viviana S. Fluxà and Noélie Maillard, Chem. Commun., 2009 , 34
DOI: 10.1039/b813732c

The biosynthetic gene cluster of zorbamycin, a member of the bleomycin family of antitumor antibiotics, from Streptomyces flavoviridis ATCC 21892
Ute Galm, Evelyn Wendt-Pienkowski, Liyan Wang, Nicholas P. George, Tae-Jin Oh, Fan Yi, Meifeng Tao, Jane M. Coughlin and Ben Shen, Mol. BioSyst., 2009 , 5 , 77
DOI: 10.1039/b814075h

STICS: surface-tethered iterative carbohydrate synthesis
Papapida Pornsuriyasak, Sneha C. Ranade, Aixiao Li, M. Cristina Parlato, Charles R. Sims, Olga V. Shulga, Keith J. Stine and Alexei V. Demchenko, Chem. Commun., 2009 , 1834
DOI: 10.1039/b817684a

Chemoenzymatic syntheses of carbasugar analogues of nucleoside diphosphate sugars: UDP-carba-Gal, UDP-carba-GlcNAc, UDP-carba-Glc, and GDP-carba-Man
Kyung-Chang Seo, Young-Geol Kwon, Dae-Hee Kim, In-Sook Jang, Jin-Won Cho and Sung-Kee Chung, Chem. Commun., 2009 , 1733
DOI: 10.1039/b821058f

Structure of the Michaelis complex of β-mannosidase, Man2A, provides insight into the conformational itinerary of mannoside hydrolysis
Wendy A. Offen, David L. Zechel, Stephen G. Withers, Harry J. Gilbert and Gideon J. Davies, Chem. Commun., 2009 , 2484
DOI: 10.1039/b902240f

Immunotherapy for cancer: synthetic carbohydrate-based vaccines
Therese Buskas, Pamela Thompson and Geert-Jan Boons, Chem. Commun., 2009 , 5335
DOI: 10.1039/b908664c

Stereoselective glycosylation using oxathiane glycosyl donors
Martin A. Fascione, Sophie J. Adshead, Susanne A. Stalford, Colin A. Kilner, Andrew G. Leach and W. Bruce Turnbull, Chem. Commun., 2009 , 5841
DOI: 10.1039/b913308a